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dc.contributor.authorHONG, JH-
dc.contributor.authorHAN, JS-
dc.contributor.authorLEE, GH-
dc.contributor.authorJUNG, IN-
dc.date.accessioned2024-01-21T23:05:38Z-
dc.date.available2024-01-21T23:05:38Z-
dc.date.created2021-09-02-
dc.date.issued1992-10-06-
dc.identifier.issn0022-328X-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/146372-
dc.description.abstractFlash vacuum pyrolysis of bis(trimethylsilylmethyl)methoxysilanes was found to be an efficient route to 1,3-disilacyclobutanes. Flash vacuum pyrolysis of bis(trimethylsilylmethyl)dimethoxysilane or bis(trimethylsilylmethyl)chloromethoxysilane gave 1-methoxy-1,3,3-trimethyl-1,3-disilacyclobutane or 1-chloro-1,3,3-trimethyl-1,3-disilacyclobutane, respectively. The thermolysis is regarded as proceeding through initial beta-elimination of trimethylmethoxysilane followed by intramolecular cyclization of the resulting 2-methoxy-4,4-dimethyl-2,4-disilapent-1-ene or 2-chloro-4,4-dimethyl-2,4-disilapent-1-ene to give the products.-
dc.languageEnglish-
dc.publisherELSEVIER SCIENCE SA LAUSANNE-
dc.titleA CONVENIENT SYNTHESIS OF 1,3-DISILACYCLOBUTANES-
dc.typeArticle-
dc.identifier.doi10.1016/0022-328X(92)85073-6-
dc.description.journalClass1-
dc.identifier.bibliographicCitationJOURNAL OF ORGANOMETALLIC CHEMISTRY, v.437, no.3, pp.265 - 270-
dc.citation.titleJOURNAL OF ORGANOMETALLIC CHEMISTRY-
dc.citation.volume437-
dc.citation.number3-
dc.citation.startPage265-
dc.citation.endPage270-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosidA1992JT13200001-
dc.identifier.scopusid2-s2.0-0344247485-
dc.relation.journalWebOfScienceCategoryChemistry, Inorganic & Nuclear-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordAuthororganosilane-
dc.subject.keywordAuthorpyrolysis-
dc.subject.keywordAuthor1,3-disilacyclobutane-
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